WO2010149437A1 - Hair conditioning composition based on c16-c22 anionic surfactant and c16-c22 fatty material - Google Patents

Hair conditioning composition based on c16-c22 anionic surfactant and c16-c22 fatty material Download PDF

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Publication number
WO2010149437A1
WO2010149437A1 PCT/EP2010/056986 EP2010056986W WO2010149437A1 WO 2010149437 A1 WO2010149437 A1 WO 2010149437A1 EP 2010056986 W EP2010056986 W EP 2010056986W WO 2010149437 A1 WO2010149437 A1 WO 2010149437A1
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WO
WIPO (PCT)
Prior art keywords
acid
anionic surfactant
composition
carbons
fatty material
Prior art date
Application number
PCT/EP2010/056986
Other languages
French (fr)
Inventor
Andrew Malcolm Murray
Thuy-Anh Pham
Original Assignee
Unilever Plc
Unilever N.V.
Hindustan Unilever Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Unilever Plc, Unilever N.V., Hindustan Unilever Limited filed Critical Unilever Plc
Publication of WO2010149437A1 publication Critical patent/WO2010149437A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/342Alcohols having more than seven atoms in an unbroken chain
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/463Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate

Definitions

  • the present invention relates to a hair conditioning composition comprising a quat-free conditioning gel.
  • the present invention relates to a hair care composition
  • a hair care composition comprising a gel network of an anionic surfactant with an alkyl group having from 16-22 carbons and a fatty material having from 16-22 carbons and water, wherein the composition comprises less than 1 % wt. anionic surfactant having an alkyl group with from 8-14 carbons and less than 0.5% wt. cationic surfactant.
  • composition is an effective conditioning composition yet comprises no quaternary ammonium surfactant.
  • the composition comprises no anionic surfactant having an alkyl group with from 8 to 14 carbons. This provides stability to the gel network within the composition.
  • the composition comprises no cationic surfactant.
  • the composition of the invention comprises a gel network comprising the anionic surfactant and the fatty material.
  • the gel network is manufactured in advance of mixing with the remaining ingredients of the composition.
  • the composition comprises an anionic hair or scalp active.
  • anionic hair or scalp actives include keratin fraction, acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, isovaleric acid, pivalic acid, oxalic acid, malonic acid, succinic acid, glutahc acid, glyceric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, propiolic acid, crotonic acid, isocrotonic acid, elaidic acid, maleic acid, fumaric acid, (N-(2,4-dihydroxy-3,3- dimethylbutyryl)- ⁇ -alanine), muconic acid, citraconic acid, mesaconic acid, camphor
  • keratin fraction is S-sulphonated, it is further preferred where the S-sulfonated keratin protein fraction is intact.
  • Intact refers to proteins that have not been significantly hydrolysed. Of particular relevance for this invention are “intact” proteins described by Gillespie in Gillespie (Biochemistry and physiology of the skin, vol. 1 , Ed. Goldsmith Oxford University Press, London,
  • keratin protein fraction is a purified form of keratin that contains predominantly, although not entirely, one distinct protein group.
  • S-Sulfonated keratins have cysteine/cystine present predominantly in the form S- sulfocysteine, commonly known as the Bunte salt.
  • Preferred keratin fractions are S-sulphonated keratin fractions containing S- sulphonated keratin high sulphur protein (SHSP). These proteins preferably have a molecular weight in the range 10-30 kD and a cysteine content determined through amino acid analysis of greater than 10%.
  • This material may be prepared by a variety of methods including those described in WO2003011894 A1.
  • the level of keratin fraction in the composition is at least 0.5 wt% of the composition (composition 1 ), preferably grater than 1 wt%, more preferably greater than 2 wt%, most preferably from 2.5 to 7 wt%.
  • the composition comprises vegetable oils.
  • vegetable oils include jojoba, soybean, sunflower seed oil, rice bran, avocado, almond, olive, sesame, castor, coconut, mink oils
  • the composition comprises anionic polymer.
  • anionic polymer examples include alkyl vinyl ether-maleic acid copolymers (Trade name: Gantrez S95), Xanthan Gum (Trade Name: Keltrol RD) and Dehydroxanthan gum (Trade Name: Amaze XT).
  • the composition has a pH of from 2.5 to 8.
  • the present invention provides the use of a composition according to any preceding claim for conditioning the hair.
  • composition according to the invention may contain any of a number of ingredients commonly found in conditioning compositions for example silicones, fatty alcohols, fatty acids, fatty amides, colourants, dyes, pigments, pearlescers, thickeners, structurants, opacifiers, etc. -A-
  • the following is a process for making a conditioning composition.
  • the different fatty materials can be co-melted together before adding into the heated water along with the anionic surfactant.

Abstract

Hair care composition comprising a gel network of an anionic surfactant with an alkyl groups with from 16-22 carbons and a fatty material having from 16-22 carbons and water, wherein the composition comprises less than 1% wt. anionic surfactant having an alkyl group with from 8-14 carbons and less than 0.5% wt. cationic surfactant.

Description

HAIR CONDITIONING COMPOSITION BASED ON C16-C22 ANIONIC SURFACTANT AND C16-C22 FATTY MATERIAL
The present invention relates to a hair conditioning composition comprising a quat-free conditioning gel.
Despite the prior art there remains the need for dedicated and effective conditioning compositions which do not comprise quaternary ammonium compounds.
Accordingly, the present invention relates to a hair care composition comprising a gel network of an anionic surfactant with an alkyl group having from 16-22 carbons and a fatty material having from 16-22 carbons and water, wherein the composition comprises less than 1 % wt. anionic surfactant having an alkyl group with from 8-14 carbons and less than 0.5% wt. cationic surfactant.
The composition is an effective conditioning composition yet comprises no quaternary ammonium surfactant.
Preferably, the composition comprises no anionic surfactant having an alkyl group with from 8 to 14 carbons. This provides stability to the gel network within the composition.
Preferably, the composition comprises no cationic surfactant.
The composition of the invention comprises a gel network comprising the anionic surfactant and the fatty material. In this regard it is essential that the gel network is manufactured in advance of mixing with the remaining ingredients of the composition. Preferably, the composition comprises an anionic hair or scalp active. Preferred anionic hair or scalp actives include keratin fraction, acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, isovaleric acid, pivalic acid, oxalic acid, malonic acid, succinic acid, glutahc acid, glyceric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, propiolic acid, crotonic acid, isocrotonic acid, elaidic acid, maleic acid, fumaric acid, (N-(2,4-dihydroxy-3,3- dimethylbutyryl)-β-alanine), muconic acid, citraconic acid, mesaconic acid, camphoric acid, benzoic acid, o, m, p-phthalic acid, naphthoic acid, toluic acid, hydratropic acid, atropic acid, cinnamic acid, isonicotinic acid, nicotinic acid, bicarbamic acid, 4,4'-dicyano-6,6'-binicotinic acid, 8-carbamoyloctanoic acid, 1 ,2,4-pentathcarboxylic acid, 2-pyrrolecarboxylic acid, 1 ,2,4,6,7- naphthalinepentaacetic acid, malonaldehydic acid, 4-hydroxyphthalamic acid, 1 - pyrazolecarboxylic acid, gallic acid or propanethcarboxylic acid and mixtures thereof.
It is preferred that keratin fraction is S-sulphonated, it is further preferred where the S-sulfonated keratin protein fraction is intact. "Intact" refers to proteins that have not been significantly hydrolysed. Of particular relevance for this invention are "intact" proteins described by Gillespie in Gillespie (Biochemistry and physiology of the skin, vol. 1 , Ed. Goldsmith Oxford University Press, London,
1983, pp475-510). These are equivalent to the keratin proteins in their native form without the disulfide cross-links formed through the process of keratinisation.
A "keratin protein fraction" is a purified form of keratin that contains predominantly, although not entirely, one distinct protein group.
S-Sulfonated keratins have cysteine/cystine present predominantly in the form S- sulfocysteine, commonly known as the Bunte salt. Preferred keratin fractions are S-sulphonated keratin fractions containing S- sulphonated keratin high sulphur protein (SHSP). These proteins preferably have a molecular weight in the range 10-30 kD and a cysteine content determined through amino acid analysis of greater than 10%. This material may be prepared by a variety of methods including those described in WO2003011894 A1.
The level of keratin fraction in the composition is at least 0.5 wt% of the composition (composition 1 ), preferably grater than 1 wt%, more preferably greater than 2 wt%, most preferably from 2.5 to 7 wt%.
Preferably, the composition comprises vegetable oils. Preferred vegetable oils include jojoba, soybean, sunflower seed oil, rice bran, avocado, almond, olive, sesame, castor, coconut, mink oils
Preferably, the composition comprises anionic polymer. Examples of anionic polymer include alkyl vinyl ether-maleic acid copolymers (Trade name: Gantrez S95), Xanthan Gum (Trade Name: Keltrol RD) and Dehydroxanthan gum (Trade Name: Amaze XT).
Preferably, the composition has a pH of from 2.5 to 8.
In a second aspect the present invention provides the use of a composition according to any preceding claim for conditioning the hair.
The composition according to the invention may contain any of a number of ingredients commonly found in conditioning compositions for example silicones, fatty alcohols, fatty acids, fatty amides, colourants, dyes, pigments, pearlescers, thickeners, structurants, opacifiers, etc. -A-
EXAMPLE 1
The following are conditioning compositions.
Figure imgf000005_0001
Figure imgf000005_0002
Figure imgf000006_0001
Figure imgf000006_0002
Figure imgf000007_0001
Figure imgf000007_0002
Figure imgf000008_0001
Figure imgf000008_0002
Figure imgf000009_0001
EXAMPLE 2
The following is a process for making a conditioning composition.
Heat water to about 700C. To this, add the polymers (when present), fatty alcohol, anionic surfactant (Sodium Cetylstearyl sulphate), using high speed stirring. When uniform dispersion obtained, cool this mixture down to about 45°C with the same speed stirring. Remaining components are then added to this with moderate speed stirring. Hair or scalp actives such as Keratec or salicylic acid and/or natural oils can be added either at the early stage when heating water (before adding fatty alcohol) or at the late stage after the mixture cooled down to about 45°C.
For better mixtures of different fatty amphiphiles, the different fatty materials can be co-melted together before adding into the heated water along with the anionic surfactant.

Claims

1. Hair care composition comprising a gel network of an anionic surfactant with an alkyl groups with from 16-22 carbons and a fatty material having from 16-22 carbons and water, wherein the composition comprises less than 1 % wt. anionic surfactant having an alkyl group with from 8-14 carbons and less than 0.5% wt. cationic surfactant.
2. Composition according to claim 1 comprising an anionic hair or scalp active.
3. Composition according to claim 1 comprising anionic polymer.
4. Composition according to any preceding claim which has a pH of from 2.5 to 8.
5. Use of a composition according to any preceding claim for conditioning the hair.
PCT/EP2010/056986 2009-06-24 2010-05-20 Hair conditioning composition based on c16-c22 anionic surfactant and c16-c22 fatty material WO2010149437A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP09163564 2009-06-24
EP09163564.9 2009-06-24

Publications (1)

Publication Number Publication Date
WO2010149437A1 true WO2010149437A1 (en) 2010-12-29

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WO (1) WO2010149437A1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013092118A1 (en) 2011-12-20 2013-06-27 Unilever N.V. Method for production of structured liquid and structured liquid
WO2021233614A1 (en) * 2020-05-20 2021-11-25 Unilever Ip Holdings B.V. Compositions and methods for providing scalp care benefits
WO2021234055A1 (en) * 2020-05-20 2021-11-25 Unilever Ip Holdings B.V. Compositions and methods for providing skin care benefits

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4736067A (en) * 1983-09-08 1988-04-05 L'oreal New dimethyl derivatives of 3-nitro-4-aminoaniline, process for their preparation and their use for dyeing keratinic fibers
US5885561A (en) * 1996-03-16 1999-03-23 Wella Aktiengesellschaft Wax combination and cosmetic compositions containing same
WO2003011894A1 (en) 2001-07-17 2003-02-13 Keratec Limited The production of soluble keratin derivatives
WO2004047774A1 (en) * 2002-11-28 2004-06-10 Keratec Limited Personal care formulations containing keratin
EP1584323A1 (en) * 2004-04-08 2005-10-12 Wella Aktiengesellschaft Use of N-hydroxyalkyl-O-benzylchitosans in hair treatment
US20060269501A1 (en) * 2002-06-04 2006-11-30 Johnson Eric S Shampoo containing a gel network
WO2009072027A2 (en) * 2007-12-07 2009-06-11 The Procter & Gamble Company Shampoo containing a gel network

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4736067A (en) * 1983-09-08 1988-04-05 L'oreal New dimethyl derivatives of 3-nitro-4-aminoaniline, process for their preparation and their use for dyeing keratinic fibers
US5885561A (en) * 1996-03-16 1999-03-23 Wella Aktiengesellschaft Wax combination and cosmetic compositions containing same
WO2003011894A1 (en) 2001-07-17 2003-02-13 Keratec Limited The production of soluble keratin derivatives
US20060269501A1 (en) * 2002-06-04 2006-11-30 Johnson Eric S Shampoo containing a gel network
WO2004047774A1 (en) * 2002-11-28 2004-06-10 Keratec Limited Personal care formulations containing keratin
EP1584323A1 (en) * 2004-04-08 2005-10-12 Wella Aktiengesellschaft Use of N-hydroxyalkyl-O-benzylchitosans in hair treatment
WO2009072027A2 (en) * 2007-12-07 2009-06-11 The Procter & Gamble Company Shampoo containing a gel network

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013092118A1 (en) 2011-12-20 2013-06-27 Unilever N.V. Method for production of structured liquid and structured liquid
WO2021233614A1 (en) * 2020-05-20 2021-11-25 Unilever Ip Holdings B.V. Compositions and methods for providing scalp care benefits
WO2021234055A1 (en) * 2020-05-20 2021-11-25 Unilever Ip Holdings B.V. Compositions and methods for providing skin care benefits

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